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Open Access Highly Accessed Research article

The FTO (fat mass and obesity associated) gene codes for a novel member of the non-heme dioxygenase superfamily

Luis Sanchez-Pulido1* and Miguel A Andrade-Navarro234

Author Affiliations

1 Centro Nacional de Biotecnologia, CSIC, Madrid, Spain

2 Molecular Medicine, Ottawa Health Research Institute, Ottawa, Canada

3 Faculty of Medicine, University of Ottawa, Ottawa, Canada

4 Max Delbrück Center for Molecular Medicine, Berlin, Germany

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BMC Biochemistry 2007, 8:23  doi:10.1186/1471-2091-8-23

Published: 8 November 2007

Abstract

Background

Genetic variants in the FTO (fat mass and obesity associated) gene have been associated with an increased risk of obesity. However, the function of its protein product has not been experimentally studied and previously reported sequence similarity analyses suggested the absence of homologs in existing protein databases. Here, we present the first detailed computational analysis of the sequence and predicted structure of the protein encoded by FTO.

Results

We performed a sequence similarity search using the human FTO protein as query and then generated a profile using the multiple sequence alignment of the homologous sequences. Profile-to-sequence and profile-to-profile based comparisons identified remote homologs of the non-heme dioxygenase family.

Conclusion

Our analysis suggests that human FTO is a member of the non-heme dioxygenase (Fe(II)- and 2-oxoglutarate-dependent dioxygenases) superfamily. Amino acid conservation patterns support this hypothesis and indicate that both 2-oxoglutarate and iron should be important for FTO function. This computational prediction of the function of FTO should suggest further steps for its experimental characterization and help to formulate hypothesis about the mechanisms by which it relates to obesity in humans.